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      Vocal divergence is concordant with genomic evidence for strong reproductive isolation in grasshopper mice ( Onychomys)

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          Abstract

          Behavioral barriers to gene flow often evolve faster than intrinsic incompatibilities and can eliminate the opportunity for hybridization between interfertile species. While acoustic signal divergence is a common driver of premating isolation in birds and insects, its contribution to speciation in mammals is less studied. Here we characterize the incidence of, and potential barriers to, hybridization among three closely related species of grasshopper mice (genus Onychomys). All three species use long‐distance acoustic signals to attract and localize mates; Onychomys arenicola and Onychomys torridus are acoustically similar and morphologically cryptic whereas Onychomys leucogaster is larger and acoustically distinct. We used genotyping‐by‐sequencing (GBS) to test for evidence of introgression in 227 mice from allopatric and sympatric localities in the western United States and northern Mexico. We conducted laboratory mating trials for all species pairs to assess reproductive compatibility, and recorded vocalizations from O. arenicola and O. torridus in sympatry and allopatry to test for evidence of acoustic character displacement. Hybridization was rare in nature and, contrary to prior evidence for O. torridus/ O. arenicola hybrids, only involved O. leucogaster and O. arenicola. In contrast, laboratory crosses between O. torridus and O. arenicola produced litters whereas O. leucogaster and O. arenicola crosses did not. Call fundamental frequency in O. torridus and O. arenicola was indistinguishable in allopatry but significantly differentiated in sympatry, a pattern consistent with reproductive character displacement. These results suggest that assortative mating based on a long‐distance signal is an important isolating mechanism between O. torridus and O. arenicola and highlight the importance of behavioral barriers in determining the permeability of species boundaries.

          Abstract

          Divergence in behavioral traits is fundamental to the evolution of reproductive isolation and maintenance of species barriers. We characterized the incidence of, and potential barriers to, hybridization among three closely related species of grasshopper mice (genus Onychomys). We found little evidence for hybridization and a signature of reproductive character displacement in the mate attractions calls of the species pair with highest ecological and morphological overlap, highlighting the importance of behavioral barriers in determining the permeability of species boundaries.

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          Sexual Selection, Social Competition, and Speciation

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            The genomics of speciation-with-gene-flow.

            The emerging field of speciation genomics is advancing our understanding of the evolution of reproductive isolation from the individual gene to a whole-genome perspective. In this new view it is important to understand the conditions under which 'divergence hitchhiking' associated with the physical linkage of gene regions, versus 'genome hitchhiking' associated with reductions in genome-wide rates of gene flow caused by selection, can enhance speciation-with-gene-flow. We describe here a theory predicting four phases of speciation, defined by changes in the relative effectiveness of divergence and genome hitchhiking, and review empirical data in light of the theory. We outline future directions, emphasizing the need to couple next-generation sequencing with selection, transplant, functional genomics, and mapping studies. This will permit a natural history of speciation genomics that will help to elucidate the factors responsible for population divergence and the roles that genome structure and different forms of hitchhiking play in facilitating the genesis of new biodiversity. Copyright © 2012 Elsevier Ltd. All rights reserved.
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              Guidelines for estimating repeatability

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                Author and article information

                Contributors
                polly.campbell@ucr.edu
                Journal
                Ecol Evol
                Ecol Evol
                10.1002/(ISSN)2045-7758
                ECE3
                Ecology and Evolution
                John Wiley and Sons Inc. (Hoboken )
                2045-7758
                06 November 2019
                November 2019
                : 9
                : 22 ( doiID: 10.1002/ece3.v9.22 )
                : 12886-12896
                Affiliations
                [ 1 ] Department of Integrative Biology Oklahoma State University Stillwater OK USA
                [ 2 ] Department of Evolution, Ecology, and Organismal Biology University of California, Riverside Riverside CA USA
                [ 3 ] Department of Developmental Pathology University of Bonn Bonn Germany
                [ 4 ] Department of Biochemistry and Molecular Biology Oklahoma State University Stillwater OK USA
                [ 5 ] Department of Forest and Conservation Sciences Forest Science Centre The University of British Columbia Vancouver BC Canada
                [ 6 ] Department of Biology The University of Oklahoma Norman OK USA
                [ 7 ] Macaulay Library Cornell Lab of Ornithology Cornell University Ithaca NY USA
                [ 8 ] Department of Neurobiology and Behavior Cornell University Ithaca NY USA
                [ 9 ] Department of Ecology and Evolutionary Biology Cornell University Ithaca NY USA
                [ 10 ] Department of Biological Sciences Northern Arizona University Flagstaff AZ USA
                Author notes
                [*] [* ] Correspondence

                Polly Campbell, Department of Evolution, Ecology, and Organismal Biology, University of California Riverside, Riverside, CA 92521, USA.

                Email: polly.campbell@ 123456ucr.edu

                Author information
                https://orcid.org/0000-0001-7660-9814
                Article
                ECE35770
                10.1002/ece3.5770
                6875671
                31788222
                50a26109-35b4-4e37-9d12-5c08da83091c
                © 2019 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 29 July 2019
                : 19 September 2019
                : 24 September 2019
                Page count
                Figures: 4, Tables: 1, Pages: 11, Words: 8327
                Funding
                Funded by: NSF‐IOS
                Award ID: 1558109
                Award ID: 1755429
                Categories
                Original Research
                Original Research
                Custom metadata
                2.0
                November 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.2 mode:remove_FC converted:25.11.2019

                Evolutionary Biology
                acoustic communication,behavioral isolation,contact zone,hybridization,reproductive character displacement,speciation

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